| Background: : Benign prostatic hyperplasia (BPH) is a common condition in aging men, often presenting with lower urinary tract symptoms, such as frequency, urgency, and nocturia. Tamsulosin and Alfuzosin, α1-adrenergic receptor antagonists, are among the primary pharmacological treatments. The current prospective study aimed to assess the safety and effectiveness of tamsulosin and alfuzosin in patients with BPH without dosage titration over a period of 4 weeks. Methods: A total of 52 patients were involved in this study, presenting with irritative symptoms of BPH and aged 45 years and above. Participants were then divided into two groups: the Tamsulosin group (26 participants), who received tamsulosin 0.4 mg, and the alfuzosin group (26 participants), who received alfuzosin 10 mg. The irritative score of the International Prostate Symptom Score (IPSS) questionnaire was used to assess the participants, in addition to the post-void residual volume (PVRV) by ultrasonography. Results: Baseline characteristics, including PVRV, were similar between groups. Tamsulosin and alfuzosin reduce BPH irritative symptoms similarly. Both significantly reduce frequency, urgency, and nocturia (p < 0.0001). However, the study compared change scores between groups; tamsulosin showed a greater mean reduction in PVRV than alfuzosin on between-group testing. Side effects were minimal; 4% of patients in the alfuzosin group experienced hypotension, and 4% reported sexual dysfunction, while no side effects were observed in the tamsulosin group. Conclusion: Treatment with tamsulosin or alfuzosin demonstrates significant improvement in the irritative symptoms of BPH, with both drugs showing comparable efficacy, while a numerically greater reduction in PVRV is observed with tamsulosin. No significant side effects were reported that affected the tolerability of either medication. |
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